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991.
In a recent paper, the first author introduced a general theory of corner rings in noncommutative rings that generalized the classical theory of Peirce decompositions. This theory is applied here to the study of the stable range of rings upon descent to corner rings. A ring is called quasi-duo if every maximal 1-sided ideal is 2-sided. Various new characterizations are obtained for such rings. Using some of these characterizations, we prove that, if a quasi-duo ring R has stable range ?n, the same is true for any semisplit corner ring of R. This contrasts with earlier results of Vaserstein and Warfield, which showed that the stable range can increase unboundedly upon descent to (even) Peirce corner rings. 相似文献
992.
Liying Wang Xingzhong Zhao Jiwen Feng 《Journal of Polymer Science.Polymer Physics》2006,44(12):1714-1724
The effects of electron irradiation on the molecular chemical structure, conformation, mobility, and phase transition of vinylidene fluoride (VDF) and trifluoroethylene (TrFE) copolymer have been investigated with variable‐temperature, solid‐state 19F nuclear magnetic resonance (NMR). It has been found that electron irradiation converts all‐trans conformations of both VDF‐rich and TrFE‐containing segments into dynamically mixed trans–gauche conformations accompanied by a simultaneous ferroelectric‐to‐paraelectric (or amorphous) transition. The variable‐temperature 19F magic‐angle‐spinning spectra results show that the paraelectric phase melts at much lower temperatures in irradiated films than in an unirradiated sample. Moreover, 19F NMR relaxation data (spin–lattice relaxation times in both the laboratory and rotating frames) reveal that electron irradiation enhances the molecular motion in paraelectric regions, whereas the molecular motion in a high‐temperature amorphous melt (>100 °C) is more constrained in irradiated films. Besides these physical changes, electron irradiation also induces the formation of several CF3 groups. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 1714–1724, 2006 相似文献
993.
non-expansive hashing scheme, similar inputs are stored in memory locations which are close. We develop a non-expansive hashing scheme
wherein any set of size from a large universe may be stored in a memory of size (any , and ), and where retrieval takes operations. We explain how to use non-expansive hashing schemes for efficient storage and retrieval of noisy data. A dynamic
version of this hashing scheme is presented as well.
Received: February 5, 1996 相似文献
994.
Martin Lorenz 《Commentarii Mathematici Helvetici》1994,69(1):474-482
LetG be a finite group acting by automorphisms on an algebraS over some commutative ringk. We show that if the action ofG restricted to the center ofS is Galois in the sense of [C-H-R], thenHH
*(S
G)≊HH
*
(S)
G. An analogous result holds for cyclic homology, provided the order ofG is invertible ink.
The author was supported in part by a grant from the NSF. 相似文献
995.
In this paper we develop some identities involving symmetric products in an abstract algebra which was formerly introduced by Rimark Ree to investigate the shuffle product and relations with skew symmetric (Lie) products. His motivation was partially the characterization of homogeneous Lie polynomials in noncommuting variables, while our motivation is derived from problems in systems theory. The main link in these applications is the need for identities involving multiple integrals of functions of many variables. The relation between these identities and some of the abstract identities developed here is also worked out and some of the applications to systems theory reviewed. 相似文献
996.
The macroscopic dynamics of a kinetic equation involving a model wave-particle collision operator of plasma physics is investigated.
The Chapman-Enskog asymptotics is first considered in the framework of a hydrodynamic scaling. The obtained macroscopic model
still involves a kinetic variable, the particle energy in the rest frame of the fluid, but shares similarities with the compressible
Navier-Stokes equation of gas dynamics. Then a diffusive scaling is examined under the hypothesis of small perturbations of
a global equilibrium. In this case, the macroscopic model couples the usual incompressible Navier-Stokes with a diffusion
equation for the energy distribution function of the particles, constrained by an extended version of the Boussinesq relation.
In both cases, the effect of a Lorentz force term is developed, in the perspective of plasma physical modelling.
Received June 16, 1997 相似文献
997.
Cytochrome P450s are a superfamily of heme monooxygenases which catalyze a wide range of biochemical reactions. The reactions involve the introduction of an oxygen atom into an inactivated carbon of a compound which is essential to produce an intermediate of a hydroxylated product. The diversity of chemical reactions catalyzed by cytochrome P450s has led to their increased demand in numerous industrial and biotechnology applications. A recent study showed that a gene sequence encoding a CYP was found in the genome of Bacillus lehensis G1, and this gene shared structural similarity with the bacterial vitamin D hydroxylase (Vdh) from Pseudonocardia autotrophica. The objectives of present study was to mine, for a novel CYP from a new isolate B. lehensis G1 alkaliphile and determine the biological properties and functionalities of CYP in this bacterium. Our study employed the usage of computational methods to search for the novel CYP from CYP structural databases to identify the conserved pattern, functional domain and sequence properties of the uncharacterized CYP from B. lehensis G1. A computational homology model of the protein’s structure was generated and a docking analysis was performed to provide useful structural knowledge on the enzyme’s possible substrate and their interaction. Sequence analysis indicated that the newly identified CYP, termed CYP107CB2, contained the fingerprint heme binding sequence motif FxxGxxxCxG at position 336-345 as well as other highly conserved motifs characteristic of cytochrome P450 proteins. Using docking studies, we identified Ser-79, Leu-81, Val-231, Val-279, Val-383, Ala-232, Thr-236 and Thr-283 as important active site residues capable of stabilizing interactions with several potential substrates, including vitamin D3, 25-hydroxyvitamin D3 and 1α-hydroxyvitamin D3, in which all substrates docked proximally to the enzyme’s heme center. Biochemical analysis indicated that CYP107CB2 is a biologically active protein to produce 1α,25-dihydroxyvitamin D3 from 1α-hydroxyvitamin D3. Based on these results, we conclude that the novel CYP107CB2 identified from B. lehensis G1 is a putative vitamin D hydroxylase which is possibly capable of catalyzing the bioconversion of parental vitamin D3 to calcitriol, or related metabolic products. 相似文献
998.
999.
《Angewandte Chemie (International ed. in English)》2017,56(14):4061-4064
The reaction of cyclo ‐P4Mes4C(NCy) ( 1 ) with two equivalents of [AuCl(tht)] (tht=tetrahydrothiophene) resulted in the formation of unusual sixteen‐membered Au–P macrocycle 2 . This macrocycle contains diphospha(III)guanidinate as a coordinating ligand, which is formed by P−P bond cleavage of 1 . Macrocycle 2 was characterized by multinuclear NMR spectroscopy, mass spectrometry and X‐ray crystallography. 相似文献
1000.
《Macromolecular bioscience》2017,17(8)
Upper Gastrointestinal Cancers (UGCs) are a leading cause of cancer‐related deaths worldwide. Paclitaxel (PTX) is frequently used for the treatment of UGCs; however, low bioavailability, reduced solubility, and dose‐dependent toxicity impede its therapeutic use. PAMAMG4.0‐NH2‐DHA is synthesized by linking amine‐terminated fourth‐generation poly(amidoamine) (PAMAMG4.0‐NH2) dendrimers with omega‐3 fatty acid docosahexaenoic acid (DHA). Next, PAMAMG4.0‐NH2‐DHA‐PTX (DHATX) and PAMAMG4.0‐NH2‐PTX (PAX) conjugates are synthesized by subsequent covalent binding of PTX with PAMAMG4.0‐NH2‐DHA and PAMAMG4.0‐NH2, respectively. 1H‐NMR and MALDI‐TOF analyses are performed to confirm conjugation of DHA to PAMAMG4.0‐NH2 and PTX to PAMAMG4.0‐NH2‐DHA. The cell viability, clonogenic cell survival, and flow cytometry analyses are used to determine the anticancer activity of PTX, PAX, and DHATX in UGC cell lines. The in vitro data indicate that treatment with DHATX is significantly more potent than PTX or PAX at inhibiting cellular proliferation, suppressing long‐term survival, and inducing cell death in UGC cells.